SUMMARY, CONCLUSIONS, AND RECOMMENDATIONS
This chapter presents the summary of the study, conclusions drawn from the findings and the recommendations based from the result of the study.
Restatement of the Problem The researchers wanted to find out the realizations of the patient who survived her terminal illness.
1. What is her illness?
2. What is her life story in relation to:
a. Family
b. Education
c. Occupation
d. Civil Status
3. What was her condition before, during, and after her illness?
a. Physical
b. Emotional
c. Spiritual
d. Financial
4. What is her realization in relation from:
a. Illness
b. Role in the Family
There was one (1) respondent who was involved in this study coming from Capas, Agoo, La Union. The respondent was chosen
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After
The respondent financial life turns to normal.
4. a. Illness. The respondent realized that having that kind of illness was too hard and scary knowing that her life might end any time. About death, Margaret realized that she was not yet ready and too scared to leave her loved ones. Her illness taught her to laugh more, love more and live more.
b. Role in the Family. The respondent realized that her role in their family being the eldest is very challenging. She felt that beside to her parents, she is also responsible to her younger siblings. She realized that she is weak without her family. The respondent realized that she is not alone during her illness. The support of her family, other people and God gave her the strength to fought back and overcome her illness.
Conclusion Based from the findings of the study, the following conclusions are drawn:
1. She is a teacher by profession and have been survived is a 45 years old. The respondent is a graduate of Bachelor of Science in secondary education and currently a high school teacher in one of the school in Agoo, La union. She is a Born Again Christian. The respondent had experience and survived in terminal
Death and attendant matters have been seminal topics of reflection, disputatious debate, and other modes of social discourse since the dawn of civilization and, presumably, also among the people who predate civilization. The sociology of death was now an accepted specialty area, but the growth and development of a hematological literature in this specialty continued to be very much an interdisciplinary effort, and it was still difficult to disentangle the sociological enterprise from that of other behavioral sciences. Moreover, Dying patients and their family members today also may use the time period between diagnosis and death to ensure that the memory of the decedent will persist after loss. The notion that the dying process may be used as a time to assert one’s identity was first set forth in Death and Identity, where Robert Fulton (1965) argued that ‘‘preserving rather than losing...personal identity’’ is a critical aspect of the dying process. Victor Marshall (1980) subsequently proposed that heightened awareness of one’s impending death trig- gears increased self-reflection, reminiscence, and the conscious construction of a coherent personal
Atul Gawande’s book, “Being Mortal: Medicine and What Matters in the End,” explores different themes such as, aging, death, and the mishandling of both aging and death by the medical profession’s. This book also addresses what it means to live well near the end of life. It is not just to survive, not just to be safe, not just to stay alive as long as the medical technology allows, but, according to the author it is about what living truly means to an individual. The author describes that the idea of “Being Mortal” developed as he watched his elderly father go through a steep decline in his health and the eventual death. He soon realized that during his medical education and training he was never taught how to help his patients with managing
When a patient is at the end of life it is very important to value the patients self dignity and their decisions at the mere end of their lives. The end of life care is to relieve the weight of the patient 's shoulders physically and mentally. I approve of end of life caring. Basic end of life care is summarized by improving the care of quality of life and dignity of the ill person. The important themes to good ethics of end of life care is a combination of human rights,respect,dignified care,and privacy.
The information that I gathered and understood the most, from all this reading, was that as a family member I should reduce my mother’s stress as much as possible. Therefore, I learned to cook after she came home, so that she would be able to rest instead of trying to provide the family home-cooked meals. My brother and I helped with the chores around our home as much possible. My mother worried about all of us, so I tried to lessen her burden.
A hospice provides a more suitable environment for those at the final stages of their lives compared to a hospital for a multitude of reasons. Hospice care is designed to care for all aspects of the person life; they provide physical, mental, and religious services, as well as caring for the patient’s family. Since hospice care is also available at home, the patient has the opportunity to die in familiar surroundings. On the contrary, hospital care provides primarily physical services to the patient and is focused on the patient’s disease. Also, dying in a hospital can be less pleasant because a connotation of hospitals is illness which is a negative quality compared to that of a home, where a person is surrounded by their memories and belongings.
Life and Death in Assisted Living Facilities Assisted living facilities are one of the fastest growing industries in the United States. Unfortunately, assisted living facilities have a history of being problematic. Specific cases from the movie Life and Death in Assisted Living Facilities indicates that assisted living facilities are often under staffed, poorly trained, and often admit elderly patients who are not qualified candidates for their facilities (Byker and Thompson, 2013). When taking this in to account, it is important to consider why families may admit their loved ones in to assisted living facilities.
This quote shows that even though Mairs sometimes has difficulty accepting her illness, she knows that there is a growing acceptance of people who must deal with the difficulties that she faces. This ultimately lends a hopeful and positive tone to an otherwise serious and depressing section of her essay. This contrast in tone, but general feeling of hope is key to the type of emotions that Nancy Mairs is trying to educate her readers about. Mair is successful in using multiple rhetorical strategies to connect with the reader.
In all my experiences as a nurse, I’ve realized the importance of communication, providing holistic care to an individual and empowering them with the knowledge to manage their health. When an illness strikes a person, it affects not just his body, but also his mind and spirit. The art of communication is invaluable to patient interaction and establishing a therapeutic nurse-patient relationship, that facilitate coping mechanisms for patients, moreover it prepared myself as a nurse to meet their individual needs. Furthermore, there is at the moment an insurmountable demand for survivorship care as a result of the advancement in technology and medicine, which made living beyond life expectancy possible for increasingly more people. Living after cancer treatment is not free of complications as there are acute and chronic side effects of treatment that requires constant monitoring and attention, and this information spurred me to shift my focus from palliative to survivorship care.
Imagine a close family member finding out they have cancer. Most people would be devastated, but my mom concurred through it and continued to brighten everyone’s day, D. Thesis- Even through her journey of cancer, my mom kept a smile on her face and continued to inspire people. E. Preview of Main Points- Cancer not only made my mom realize how lucky she was, but it also pushed her to become a better person.
When she had to return to chemotherapy, she was almost happy to go because it was familiar and she was accepted. She always had a companion there whether it was a doctor, nurse, or another patient. She was no longer the outcast. A lot of her time was spent criticizing “normal” people for wanting to be somebody else when all she wanted to be was like everyone else. She defined herself as an individual base on how other people saw her.
It brought to my awareness both the limitation and the capacity of medicine. Although there was no medical intervention that could cure the diseases of those terminal patients, their quality of life was improved by an outstanding team of doctors, nurses and volunteers. This awareness helped reconcile myself to the fact that certain things, such as death and terminal illness, can not be avoided or changed. By viewing death as a natural part of life, I will be able to offer my dying patients the best care possible while also understanding my limitation as a physician and a human being.
Her husband isolated her from others and her child, which caused her condition to worsen because she felt that she couldn’t care for her family as she
Everything from how her interactions with her family to her perception of her environment and how it evolves throughout the story allow the reader to almost feel what the narrator is feeling as the moves through the story. In the beginning, the only reason the reader knows there may be something wrong with the narrator is because she comes right out and says she may be ill, even though her husband didn’t believe she was (216). As the story moves on, it becomes clear that her illness is not one of a physical nature, but of an emotional or mental one. By telling the story in the narrator’s point of view, the reader can really dive into her mind and almost feel what she’s feeling.
This assignment also covers the importance of hope for patients and the role hope plays in terminally ill patients. I will also discuss ways in which health professionals can foster hope in terminally ill patients. I was on my placement on an oncology ward. It was my second week on
the theory is patient-specific because of the patient’s diagnoses and the limited verbal communication. The theory assumptions are helpful with this patient as the nurses make it a priority to interpret cues which reflect his end of life experience and giving prompt intervention to maintain peaceful experience even at his dying moment. The theory was developed be used with terminally ill adult patients and their families/significant others. The theory is not applicable in its totality with non-hospice or palliative care patients. The goal of the end of life care is not to optimize care rather is to provide comfort measures, dignity and peaceful end of life experience.